Chronic immune activation associated with chronic helminthic and human immunodeficiency virus infections: Role of hyporesponsiveness and anergy

被引:111
作者
Borkow, G
Bentwich, Z
机构
[1] Hebrew Univ Jerusalem, Fac Agr, IL-76100 Rehovot, Israel
[2] Hebrew Univ Jerusalem, Hadassah Med Sch, IL-91010 Jerusalem, Israel
关键词
D O I
10.1128/CMR.17.4.1012-1030.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Chronic immune activation is one of the hallmarks of human immunodeficiency virus (HIV) infection. It is present also, with very similar characteristics, in very large human populations infested with helminthic infections. We have tried to review the studies addressing the changes in the immune profiles and responses of hosts infected with either one of these two chronic infections. Not surprisingly, several of the immune derangements and impairments seen in HIV infection, and considered by many to be the "specific" effects of HIV, can be found in helminth-infected but HIV-noninfected individuals and can thus be accounted for by the chronic immune activation itself. A less appreciated element in chronic immune activation is the immune suppression and anergy which it may generate. Both HIV and helminth infections represent this aspect in a very wide and illustrative way. Different degrees of anew and immune hyporesponsiveness are present in these infections and probably have far-reaching effects on the ability of the host to cope with these and other infections. Furthermore, they may have important practical implications, especially with regard to protective vaccinations against AIDS, for populations chronically infected with helminths and therefore widely anergic. The current knowledge of the mechanisms responsible for the generation of anergy by chronic immune activation is thoroughly reviewed.
引用
收藏
页码:1012 / +
页数:20
相关论文
共 276 条
[1]   Functional diversity of helper T lymphocytes [J].
Abbas, AK ;
Murphy, KM ;
Sher, A .
NATURE, 1996, 383 (6603) :787-793
[2]   HELMINTH INFECTION RESULTS IN DECREASED VIRUS-SPECIFIC CD8+ CYTOTOXIC T-CELL AND TH1-CYTOKINE RESPONSES AS WELL AS DELAYED VIRUS CLEARANCE [J].
ACTOR, JK ;
SHIRAI, M ;
KULLBERG, MC ;
BULLER, RML ;
SHER, A ;
BERZOFSKY, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (03) :948-952
[3]   Decline in total serum IgE after treatment for tuberculosis [J].
Adams, JFA ;
Schölvinck, EH ;
Gie, RP ;
Potter, PC ;
Beyers, N ;
Beyers, AD .
LANCET, 1999, 353 (9169) :2030-2033
[4]   Elevated levels of circulating interleukin-18 in human immunodeficiency virus-infected individuals: Role of peripheral blood mononuclear cells and implications for AIDS pathogenesis [J].
Ahmad, R ;
Sindhu, STA ;
Toma, E ;
Morisset, R ;
Ahmad, A .
JOURNAL OF VIROLOGY, 2002, 76 (24) :12448-12456
[5]   The Ras/MAPK cascade and the control of positive selection [J].
Alberola-Ila, J ;
Hernández-Hoyos, G .
IMMUNOLOGICAL REVIEWS, 2003, 191 (01) :79-96
[6]   Inhibition of protein kinases prevents lymphocyte activation by Schistosoma mansoni antigens and reduces in vivo granuloma reaction [J].
Almeida, CA ;
Romano-Silva, MA ;
Goes, AM .
IMMUNOLOGY LETTERS, 1998, 62 (03) :137-143
[7]   Direct HIV cytopathicity cannot account for CD4 decline in AIDS in the presence of homeostasis: A worst-case dynamic analysis [J].
Anderson, RW ;
Ascher, MS ;
Sheppard, HW .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 1998, 17 (03) :245-252
[8]  
Andreassen J., 1997, Parassitologia (Rome), V39, P259
[9]  
ASCHER MS, 1988, CLIN EXP IMMUNOL, V73, P165
[10]   A schistosome-expressed immunomodulatory glycoconjugate expands peritoneal Gr1+ macrophages that suppress naive CD4+ T cell proliferation via an IFN-γ and nitric oxide-dependent mechanism [J].
Atochina, O ;
Daly-Engel, T ;
Piskorska, D ;
McGuire, E ;
Harn, DA .
JOURNAL OF IMMUNOLOGY, 2001, 167 (08) :4293-4302